Senior Associate – Evidence Synthesis, Clinical Outcome Assessments (COA)
Location: Hyderabad, India
Employment Type: Full-Time, Permanent
About Sanofi
Sanofi is an R&D-driven, AI-powered global biopharmaceutical company, committed to improving lives worldwide. Our innovative pipeline in immunology, chronic disease care, vaccines, and specialty medicines drives scientific breakthroughs that impact millions. With a focus on patient-centric innovation, Sanofi leverages digital tools, AI, and global collaboration to accelerate healthcare solutions.
Visit: www.sanofi.com
Role Overview
The Senior Associate – Evidence Synthesis, COA will contribute to the integration of patient perspectives in clinical research using Clinical Outcome Assessments (COAs). This role, based in Hyderabad, involves generating robust scientific evidence to support strategic decision-making, regulatory submissions, and value messaging across Sanofi’s global portfolio.
You will work closely with the Global COA team within the Patient-Informed Development & Health Value Translation (PID&HVT) department, supporting evidence generation and COA strategy development for products and programs worldwide.
Key Responsibilities
Evidence Synthesis & COA Strategy
Lead and contribute to evidence synthesis projects, including search strategy development, literature screening, data extraction, and COA analysis.
Conduct disease conceptual modeling and generate insights into disease and treatment paradigms using primary and secondary research.
Support development, validation, and implementation of Fit-for-Purpose COA instruments for clinical research projects.
Assist in preparation of scientific reports, regulatory dossiers, and publications for internal and external communication.
Develop and optimize COA endpoint strategies aligned with Sanofi’s Best-in-Class/First-in-Class approach.
Stakeholder Engagement
Collaborate with COA leads, HEVA, RWE, Clinical, Medical Affairs, Marketing, and Market Access teams globally and locally.
Serve as a subject matter expert (SME) for team members, providing guidance on project execution and scientific strategy.
Identify opportunities to innovate COA value identification and evidence dissemination for regulatory and reimbursement impact.
Process Improvement & Governance
Contribute to COA evidence generation templates, processes, and strategic frameworks.
Ensure compliance with FDA, EMA, and internal regulatory guidelines.
Maintain adherence to evidence generation standards, ensuring quality and scientific rigor.
Requirements
Educational Qualification:
Bachelor’s, Master’s, or PhD in Life Sciences, Clinical Research, or related fields.
Experience & Skills:
Minimum 5+ years in COA science, including COA data analyses, instrument creation/validation, or COA endpoint strategy in pharmaceuticals, CROs, or academia.
Strong analytical skills to synthesize qualitative and quantitative data and translate findings into actionable evidence strategies.
Experience in literature reviews, qualitative research, and patient-centered outcome studies.
Excellent written and verbal communication skills in English.
Ability to manage stakeholders, work independently, and guide team members.
Why Join Sanofi
Opportunity to work on global, patient-centric research initiatives in a leading biopharma company.
Exposure to AI-driven evidence generation and innovative COA methodologies.
Collaborate with cross-functional teams across clinical, regulatory, and commercial domains.
Work in a supportive and inclusive environment with a focus on career growth and skill development.
Flexible work arrangements, opportunities to attend conferences, and access to professional development programs.
Equal Opportunity Employer
Sanofi provides equal employment opportunities for all candidates, regardless of race, color, ancestry, religion, sex, sexual orientation, age, citizenship, disability, or other characteristics protected by law.
Important Notice: Sanofi does not charge applicants for employment. Any requests for payment are fraudulent.
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